NM_004960.4(FUS):c.833-29C>T AND not provided
- Germline classification:
- Benign/Likely benign (3 submissions)
- Last evaluated:
- Jul 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001593981.21
Allele description [Variation Report for NM_004960.4(FUS):c.833-29C>T]
NM_004960.4(FUS):c.833-29C>T
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens Usher syndrome 1C (autosomal recessive, severe), mRNA (cDNA clone M...
Homo sapiens Usher syndrome 1C (autosomal recessive, severe), mRNA (cDNA clone MGC:23100 IMAGE:4867369), complete cdsgi|16359184|gb|BC016057.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 20, 2024